PDS5A

PDS5 cohesin associated factor A
OMIM: 613200, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Amber PDS5A in Mendeliome


Version 2.56

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Complex neurodevelopmental disorder, MONDO:0100038, PDS5A -related

Amber PDS5A in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 2.9

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
  • Literature
  • Literature
Phenotypes
  • complex neurodevelopmental disorder, MONDO:0100038, PDS5A -related